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CysC Fast Test Kit (Imumunofluorescence Assay - India CDSCO Medical Device Registration

CysC Fast Test Kit (Imumunofluorescence Assay is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000410_cf478cc23f3713dca48c70ed4f35ba4e_0e1b2d6a6939f93e4568604188681322. This device is marketed under the brand name Imumunofluorescence Assay. The license holder is Vector Biotek Pvt Ltd, and it is classified as Device Class Class B. The approving authority is CDSCO.

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CDSCO Registered
Class Class B
CysC Fast Test Kit (Imumunofluorescence Assay
UID: IMP/IVD/2019/000410_cf478cc23f3713dca48c70ed4f35ba4e_0e1b2d6a6939f93e4568604188681322

Brand Name

Imumunofluorescence Assay

License Holder

Vector Biotek Pvt Ltd

Device Class

Class B

Approving Authority

CDSCO

Product Information

CysC Fast Test Kit (Imumunofluorescence Assay) is intended for in vitro quantitative determination of Cystatin C (Imumunofluorescence Assay) in serum, plasma or whole blood. The test result is used as an aid in the assessment and evaluation of index of glomerular filtration rate, and has important application value in renal function, kidney damage and renal transplantation

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